EMA – CTIS training updates
The EMA updated a series of its CTIS training materials:
- Guide to CTIS training material catalogue
- FAQs: How to manage a CT – CTIS Training Programme – Module 05
- FAQs: How to create, submit and withdraw a Clinical Trial Application – CTIS Training Programme – Module 10
- Step-by-step guide: Supervise a Clinical Trial: Ad Hoc Assessment – CTIS Training Programme – Module 17
- Instructor’s guide: Supervise a Clinical Trial: Ad Hoc Assessment – CTIS Training Programme – Module 17
- FAQs: Supervise a Clinical Trial: Ad Hoc Assessment – CTIS Training Programme – Module 17
- Sponsors’ guide: Transition of trials from EudraCT to CTIS – CTIS Training Programme – Module 23
- Sponsor Handbook
EMA provides an online modular training programme to help clinical trial sponsors, national competent authorities, ethics committees, European Commission and EMA staff use the Clinical Trials Information System (CTIS). The programme contains modules and audience-targeted materials covering all clinical trial lifecycle stages, from submission through authorisation to supervision.
Find more content on the CTIS online training on the EMA Website.
OpenEdition vous propose de citer ce billet de la manière suivante :
vroby (21 octobre 2024). EMA – CTIS training updates. ELSIBI. Consulté le 12 janvier 2026 à l’adresse https://doi.org/10.58079/12jhf





